IR signals for carbonyl compounds | Spectroscopy | Organic chemistry | Khan Academy

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  • Опубликовано: 24 ноя 2024

Комментарии • 16

  • @MohitKumar-sf3rc
    @MohitKumar-sf3rc 7 лет назад

    great persons like you shows that why U.S is the forward country. You are feeling country proud.

  • @fakhrulnawawi9681
    @fakhrulnawawi9681 3 года назад

    Very easy to understand thanks

  • @muhammadyounastahir1872
    @muhammadyounastahir1872 4 года назад

    Really impressive video for my understanding

  • @qaishassan8760
    @qaishassan8760 3 года назад

    Thank you so much, it’s so helpful.

  • @nackomega9505
    @nackomega9505 6 лет назад +1

    Thx bro, this video help me so much.

  • @sinagholamimalek5569
    @sinagholamimalek5569 2 года назад

    very nice thank you

  • @SomashreeSaha
    @SomashreeSaha 2 года назад

    Thank you sir

  • @melikasaffari1265
    @melikasaffari1265 4 года назад

    Great! Thank u🥰♥️

  • @pavankumarreddyyeruva1804
    @pavankumarreddyyeruva1804 4 года назад

    Thank you❤ so much it helps me more

  • @Yuvachemistry
    @Yuvachemistry 6 лет назад

    Very nice.. thank you

  • @rahulshivram5256
    @rahulshivram5256 4 года назад

    Is there any way to quantify these effects

  • @ibrammikhail8079
    @ibrammikhail8079 5 лет назад +1

    in 6:40 . I know that the resonance effect of -OR is more than the inductive effect. Please correct me.

  • @minseokhan8521
    @minseokhan8521 6 лет назад +1

    Wouldn't the inductive effect be more prominent in ester than the acyl chloride since the electronegativity of oxygen is higher than the that of chloride? Because in this sense, I think acyl chloride should be placed in a lower wavenumber than ester....can anyone help me on this?!?

  • @negoruh
    @negoruh 9 лет назад

    18.000